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Inherited defects in thyroid hormone cell-membrane transport and metabolism

The description of two novel human defects in the last ten years has uncovered new aspects of thyroid hormone physiology with regard to cellular-membrane transport and intracellular metabolism. Mutations in the X-linked monocarboxylate transporter 8 (MCT8) gene result in an invalidating neurodevelop...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Fu, Jiao, Dumitrescu, Alexandra M.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2013
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3959653/
https://ncbi.nlm.nih.gov/pubmed/24629861
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.beem.2013.05.014
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